{"id":39659,"date":"1999-01-01T00:00:00","date_gmt":"1999-01-01T00:00:00","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/estudio-de-la-homoconjugacion-aromatica-y-sus-implicaciones-en-quimica-molecular-supramolecular-y-macromolecular\/"},"modified":"1999-01-01T00:00:00","modified_gmt":"1999-01-01T00:00:00","slug":"estudio-de-la-homoconjugacion-aromatica-y-sus-implicaciones-en-quimica-molecular-supramolecular-y-macromolecular","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/quimica\/estudio-de-la-homoconjugacion-aromatica-y-sus-implicaciones-en-quimica-molecular-supramolecular-y-macromolecular\/","title":{"rendered":"Estudio de la homoconjugacion aromatica y sus implicaciones en quimica molecular, supramolecular y macromolecular."},"content":{"rendered":"<h2>Tesis doctoral de <strong> \u00c1lvaro De Fresno Cerezo <\/strong><\/h2>\n<p>En la memoria que se presenta, se estudian diversos aspectos de una serie de fen\u00f3menos relacionados con la homoconjugaci\u00f3n arom\u00e1tica y las interacciones no covalentes con sistemas arom\u00e1ticos, emple\u00e1ndose como modelo el 7,7-difenilnorbornano (dfn).  en resumen, se ha comprobado como una mol\u00e9cula relativamente sencilla y f\u00e1cilmente accesible como esta, es un sustrato idoneo para el estudio de la homoconjugaci\u00f3n arom\u00e1tica apical, las interacciones pi-pi arom\u00e1ticas cara-cara y lado-cara, las interacciones debiles debidas a puentes de hidrogeno c-h &#8230;.F-c y las interacciones oh&#8230;Pi as\u00ed como puentes de hidr\u00f3geno en nitroanilinas. tambi\u00e9n se ha puesto de manifiesto que derivados del dfn presentan propiedades \u00f3pticas no luneales. finalmente, el dfn puede ser empleado como subunidad en la s\u00edntesis de macrociclos con un elevado grado de preorganizaci\u00f3n y en la s\u00edntesis de pol\u00edmeros homoconjugados.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Estudio de la homoconjugacion aromatica y sus implicaciones en quimica molecular, supramolecular y macromolecular.<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Estudio de la homoconjugacion aromatica y sus implicaciones en quimica molecular, supramolecular y macromolecular. <\/li>\n<li><strong>Autor:<\/strong>\u00a0 \u00c1lvaro De Fresno Cerezo <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Complutense de Madrid<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 01\/01\/1999<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<h3>Direcci\u00f3n y tribunal<\/h3>\n<ul>\n<li><strong>Director de la tesis<\/strong>\n<ul>\n<li>Antonio Garcia Martinez<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: Carlos \u00e1lvarez ibarra <\/li>\n<li>Fernando Agullo lopez (vocal)<\/li>\n<li>Manuel Rico sarompes (vocal)<\/li>\n<li>enrique Teso villar (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de \u00c1lvaro De Fresno Cerezo En la memoria que se presenta, se estudian diversos aspectos de una serie [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center 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